First Concise Total Syntheses of Biologically Interesting Nicolaioidesin C,Crinatusin C1, and Crinatusin C2

The efficient and concise total syntheses of naturally occurring dihydrochalcone nicolaioidesin C, crinatusin C₁, and crinatusin C₂have been achieved from the readily available 2,6-dihydroxy-4-methoxyacetophenone and 2,4-dihydroxy-6-methoxyacetophenone. The key steps in the synthetic strategy were a...

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Veröffentlicht in:Bulletin of the Korean Chemical Society 2008, 29(6), , pp.1199-1204
Hauptverfasser: Eun Mi Jung, 이용록
Format: Artikel
Sprache:eng
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Zusammenfassung:The efficient and concise total syntheses of naturally occurring dihydrochalcone nicolaioidesin C, crinatusin C₁, and crinatusin C₂have been achieved from the readily available 2,6-dihydroxy-4-methoxyacetophenone and 2,4-dihydroxy-6-methoxyacetophenone. The key steps in the synthetic strategy were aldol reaction and Diels-Alder reaction. KCI Citation Count: 17
ISSN:0253-2964
1229-5949
DOI:10.5012/bkcs.2008.29.6.1199